DE ROBERTIS E
J Biophys Biochem Cytol. 1956 Sep 25;2(5):503-12. doi: 10.1083/jcb.2.5.503.
The degenerative changes of the synaptic regions after nerve section have been studied with the electron microscope in the interneuronal synapse of the ventral ganglion of the acoustic nerve of the guinea pig. Fixation with buffered osmic tetroxide was carried out 22, 44, and 48 hours after destruction of the cochlea on one side; the contralateral ganglion being used as control. The submicroscopic organization of normal axosomatic and axodendritic synapses is described. In the synaptic ending four morphological components are recognized: the membrane, the mitochondria, the synaptic vesicles (19, 20), and the cytoplasmic matrix. The intimate contact of glial processes with the endings and with the surface of the nerve cell is described. At the level of the synaptic junction there is a direct contact of the limiting membranes of the ending and of the cell body or dendrite. Both contacting membranes constitute the synaptic one with a total thickness of about 250 A. This membrane has regions of higher electron density where the synaptic vesicles come into intimate contact and fuse with it. Definite degenerative submicroscopic changes in the nerve endings were observed after 22 hours of destruction of the cochlea and were much more conspicuous after 44 and 48 hours. After 22 hours there is swelling of the ending and decreased electron density of the matrix. Most synaptic vesicles have disappeared or seem to undergo a process of clumping and dissolution. Some mitochondria also show signs of degeneration. After 44 hours the synaptic vesicles have practically disappeared; mitochondria are in different stages of lysis; the membrane of the ending becomes irregular in shape, and there is shrinkage and in some cases detachment of the ending. No changes in the postsynaptic cytoplasm were observed. These observations and particularly the rapid lysis of the synaptic vesicles are discussed in correlation with data from the literature indicating the early alteration of synaptic function and the biochemical changes occurring after section of the afferent nerve. The hypothesis that the synaptic vesicles may be carriers of acetylcholine or other active substances (19, 20) and that they may act as biochemical units in synaptic transmission is also discussed.(2)
用电子显微镜研究了豚鼠听神经腹侧神经节神经元间突触在神经切断后突触区域的退行性变化。在一侧耳蜗破坏后22、44和48小时,用缓冲四氧化锇进行固定;对侧神经节用作对照。描述了正常轴体和轴树突触的亚微观结构。在突触末梢可识别出四种形态学成分:膜、线粒体、突触小泡(19, 20)和细胞质基质。描述了神经胶质突起与末梢以及神经细胞表面的紧密接触。在突触连接处,末梢与细胞体或树突的限制膜直接接触。两个接触膜构成总厚度约为250埃的突触膜。该膜有电子密度较高的区域,突触小泡与之紧密接触并融合。在耳蜗破坏22小时后观察到神经末梢有明确的亚微观退行性变化,在44和48小时后更为明显。22小时后,末梢肿胀,基质电子密度降低。大多数突触小泡消失或似乎经历聚集和溶解过程。一些线粒体也显示出退化迹象。44小时后,突触小泡几乎消失;线粒体处于不同程度的溶解阶段;末梢膜形状不规则,末梢有收缩,在某些情况下有脱离。未观察到突触后细胞质的变化。结合文献数据讨论了这些观察结果,特别是突触小泡的快速溶解,这些数据表明突触功能的早期改变以及传入神经切断后发生的生化变化。还讨论了突触小泡可能是乙酰胆碱或其他活性物质的载体(19, 20)以及它们可能作为突触传递中的生化单位的假说。(2)